Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

[reaction: see text] Conformationally restricted amino alcohols based on carbohydrate scaffolds provide flexible and fine-tuneable libraries that greatly expand the range of ligands available in the Zn(OTf)(2)-mediated addition of alkynes to aldehydes, in some cases with very high stereoselectivities.

Original publication

DOI

10.1021/ol052503l

Type

Journal article

Journal

Org Lett

Publication Date

19/01/2006

Volume

8

Pages

207 - 210

Keywords

Aldehydes, Alkynes, Amino Alcohols, Carbohydrates, Combinatorial Chemistry Techniques, Ligands, Mesylates, Stereoisomerism